PubMed for id: 867208

Year	Number of Results
1991	1
1992	1
1995	1
1998	1
1999	2
2000	1
2009	1
2010	1
2012	2
2013	4
2014	1
2016	1
2018	1
2020	3
2021	4
2022	1
2024	0

1

Gyrate Atrophy of the Choroid and Retina: A Review.

Elnahry AG, Elnahry GA. Elnahry AG, et al. Eur J Ophthalmol. 2022 May;32(3):1314-1323. doi: 10.1177/11206721211067333. Epub 2021 Dec 13. Eur J Ophthalmol. 2022. PMID: 34894815 Review.

2

Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.

Kraoua I, Bouyacoub Y, Drissi C, Chargui M, Rebai I, Chebil A, Klaa H, Benrhouma H, Hassen A, Gouider-Khouja N, Abdelhak S, Boespflug-Tanguy O, Youssef-Turki IB, Dorboz I. Kraoua I, et al. Neuropediatrics. 2021 Aug;52(4):302-309. doi: 10.1055/s-0041-1728654. Epub 2021 Jun 30. Neuropediatrics. 2021. PMID: 34192786 Review.

3

Mutation of the TRPM3 cation channel underlies progressive cataract development and lens calcification associated with pro-fibrotic and immune cell responses.

Zhou Y, Bennett TM, Shiels A. Zhou Y, et al. FASEB J. 2021 Feb;35(2):e21288. doi: 10.1096/fj.202002037R. FASEB J. 2021. PMID: 33484482 Free PMC article.

4

A novel c.980C>G variant in OAT results in identifiable gyrate atrophy phenotype associated with retinal detachment in a young female.

Magliyah M, Alsalamah AK, AlOtaibi M, Nowilaty SR. Magliyah M, et al. Ophthalmic Genet. 2021 Apr;42(2):204-208. doi: 10.1080/13816810.2020.1843185. Epub 2020 Nov 26. Ophthalmic Genet. 2021. PMID: 33243052

5

Yang X, Xu J, Fu C, Jia Z, Yao K, Chen X. Yang X, et al. Biochem Biophys Res Commun. 2020 May 28;526(2):459-465. doi: 10.1016/j.bbrc.2020.03.072. Epub 2020 Mar 28. Biochem Biophys Res Commun. 2020. PMID: 32234236

6

Recurrent PAX 6 mutation in a Chinese family with congenital aniridia, progressive cataracts and mental retardation.

Chen DD, Yang T, Zhu SQ. Chen DD, et al. Eur J Ophthalmol. 2020 Jan;30(1):181-188. doi: 10.1177/1120672118810998. Epub 2018 Nov 14. Eur J Ophthalmol. 2020. PMID: 30426773

7

Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial.

Ghazi NG, Abboud EB, Nowilaty SR, Alkuraya H, Alhommadi A, Cai H, Hou R, Deng WT, Boye SL, Almaghamsi A, Al Saikhan F, Al-Dhibi H, Birch D, Chung C, Colak D, LaVail MM, Vollrath D, Erger K, Wang W, Conlon T, Zhang K, Hauswirth W, Alkuraya FS. Ghazi NG, et al. Hum Genet. 2016 Mar;135(3):327-43. doi: 10.1007/s00439-016-1637-y. Epub 2016 Jan 29. Hum Genet. 2016. PMID: 26825853 Clinical Trial.

8

Lack of dystrophin protein Dp71 results in progressive cataract formation due to loss of fiber cell organization.

Fort PE, Darche M, Sahel JA, Rendon A, Tadayoni R. Fort PE, et al. Mol Vis. 2014 Nov 4;20:1480-90. eCollection 2014. Mol Vis. 2014. PMID: 25489223 Free PMC article.

9

Novel FAM126A mutations in hypomyelination and congenital cataract disease.

Traverso M, Assereto S, Gazzerro E, Savasta S, Abdalla EM, Rossi A, Baldassari S, Fruscione F, Ruffinazzi G, Fassad MR, El Beheiry A, Minetti C, Zara F, Biancheri R. Traverso M, et al. Biochem Biophys Res Commun. 2013 Sep 27;439(3):369-72. doi: 10.1016/j.bbrc.2013.08.077. Epub 2013 Aug 30. Biochem Biophys Res Commun. 2013. PMID: 23998934

10

Structural integrity of the Greek key motif in βγ-crystallins is vital for central eye lens transparency.

Vendra VP, Agarwal G, Chandani S, Talla V, Srinivasan N, Balasubramanian D. Vendra VP, et al. PLoS One. 2013 Aug 6;8(8):e70336. doi: 10.1371/journal.pone.0070336. Print 2013. PLoS One. 2013. PMID: 23936409 Free PMC article.

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